Category: COTBC Newsletter

For many people, the winter season can be a time of joy and celebration. For others, fewer daylight hours and the demands of the holidays can leave them feeling deeply tired, lonely, overwhelmed, or irritable. This year, those feelings may be compounded by other stressors such as the impacts of the pandemic, local weather events, and travel limitations. As health care providers, it can be tempting to ‘push down’ these feelings so that we can get on with providing services for our clients.

At the College, we recognize these are extraordinary times and that people may be struggling. We encourage you to take some time to reflect on how you are doing this year and think about ways to proactively take care of yourself.

For some, this may include focusing on getting enough sleep, eating a balanced diet, engaging in mindfulness or relaxation practices, getting some exercise, or seeking out safe social activities.

For others, this may also mean reaching out for help and advice – whether from your medical practitioner, employment assistance program, or other trusted source.

If you notice a colleague seeming not quite like themselves this season, please check in with them. By taking care of yourself and supporting your colleagues to do the same, you are taking important steps to meet your professional obligations to be able to provide good care for others.

The College’s Practice Team is also available as a resource and can be reached at practice@cotbc.org.

We wish you good health!

At a recent BC Public Advisory Network meeting, staff from nine different Colleges met with members of the public to discuss the topic of informed consent. While registrants must meet their College’s Practice Standards that set out the requirements for obtaining informed consent, it was helpful to hear the client’s unique perspective. Public advisors were asked what they expect from health care professionals when it comes to informed consent. Following are highlights from the discussion on public expectations:

• Explicitly express that treatment requires their consent. Not everyone is aware that consent is needed.
• Be cautious about using family members to translate when obtaining consent for higher risk interventions, sometimes the translation isn’t accurate.
• Watch out for literacy issues if written text is being used. Consider adding diagrams. Offer pre-reading material if available.
• There are opportunities for discrimination when obtaining consent. If practitioners assume that the client cannot understand the description of the treatment, language used may not be clear, truthful, or complete.
• Do not make assumptions about the choices or preferences of the client.
• Invite the opportunity to ask questions and engage with the client.
• Be empathetic and considerate of the client’s lived experience.
• Have evidence to back up treatment suggestions. Some clients will have done online research and will expect a conversation about pros and cons of treatment options.
• Ask the client to repeat back their understanding of the treatment to ensure that the information has been understood. Reaffirm consent.

When asked why consent is important to the public, the responses were powerful:

“It’s important to take the time to get consent properly, if you have a good process, it builds trust.”

When providing consent, “… we are putting our health and wellness in the hands of a practitioner. It is our right to do so with the best possible information.”

Interested in learning more about the public advisors’ perspectives? Read the full BC-PAN meeting summary.